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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1403670Generated: October 30, 2026

Sodium Carbonate → 2'-(1-tert-Butoxycarbonylamino-ethyl)-5'-(3-fluoro-pyridin-4-ylcarbamoyl)-biphenyl-3-carboxylic acid

https://huagongshe.com/reaction/1403670

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant3-Carboxyphenylboronic acidHCID 2733957—
Reactant{1-[2-Bromo-4-(3-fluoro-pyridin-4-ylcarbamoyl)-phenyl]-ethyl}-carbamic acid tert-butyl esterHCID 67407943—
CatalystHCID 178418397HCID 178418397—
SolventCitric AcidHCID 311—
SolventWaterHCID 962—
SolventDimethoxyethane ethanol waterHCID 86587095—
Product2'-(1-tert-Butoxycarbonylamino-ethyl)-5'-(3-fluoro-pyridin-4-ylcarbamoyl)-biphenyl-3-carboxylic acidHCID 67409767—

Reaction Conditions

Temperature130 °C

Reaction Steps

To a solution of {1-[2-bromo-4-(3-fluoro-pyridin-4-ylcarbamoyl)-phenyl]-ethyl}-carbamicacid tert-butyl ester (2841 μmol) and 3-carboxyphenylboronic acid (1.5 eq.) in a mixture of DME/EtOH/water: 1/1/1 (10 ml) was added Na2CO3 (4 eq) and Pd tetrakis (0.05 eq). The reaction mixture was heated in the microwave at 130° C. for 1.5 hours. The reaction mixture was diluted with water and citric acid (to acidic pH) and extracted with EtOAc. The combined organic layers were dried over MgSO4 and the solvent was removed under reduced pressure. The compound was purified by column chromatography (silicagel, DCM/MeOH gradient).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08912209B2
Source datasetuspto-grants-2014_12
ORD IDord-fda90fd4ed6545158ee75d226cf37f77
Source noteuspto-grants-2014_12